Canonical Allele Identifier: CA16033586

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112841194T>A , CM000667.2:g.112841194T>A	GRCh38
NC_000005.9:g.112176891T>A , CM000667.1:g.112176891T>A	GRCh37
NC_000005.8:g.112204790T>A	NCBI36
NG_008481.4:g.153674T>A , LRG_130:g.153674T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000038.6:c.5600T>A MANE Select	NP_000029.2:p.Phe1867Tyr
ENST00000257430.9:c.5600T>A MANE Select	ENSP00000257430.4:p.Phe1867Tyr
NM_000038.5:c.5600T>A	NP_000029.2:p.Phe1867Tyr
NM_001127510.2:c.5600T>A	NP_001120982.1:p.Phe1867Tyr
NM_001127510.3:c.5600T>A	NP_001120982.1:p.Phe1867Tyr
NM_001127511.2:c.5546T>A	NP_001120983.2:p.Phe1849Tyr
NM_001127511.3:c.5546T>A	NP_001120983.2:p.Phe1849Tyr
NM_001354895.1:c.5600T>A	NP_001341824.1:p.Phe1867Tyr
NM_001354895.2:c.5600T>A	NP_001341824.1:p.Phe1867Tyr
NM_001354896.1:c.5654T>A	NP_001341825.1:p.Phe1885Tyr
NM_001354896.2:c.5654T>A	NP_001341825.1:p.Phe1885Tyr
NM_001354897.1:c.5630T>A	NP_001341826.1:p.Phe1877Tyr
NM_001354897.2:c.5630T>A	NP_001341826.1:p.Phe1877Tyr
NM_001354898.1:c.5525T>A	NP_001341827.1:p.Phe1842Tyr
NM_001354898.2:c.5525T>A	NP_001341827.1:p.Phe1842Tyr
NM_001354899.1:c.5516T>A	NP_001341828.1:p.Phe1839Tyr
NM_001354899.2:c.5516T>A	NP_001341828.1:p.Phe1839Tyr
NM_001354900.1:c.5477T>A	NP_001341829.1:p.Phe1826Tyr
NM_001354900.2:c.5477T>A	NP_001341829.1:p.Phe1826Tyr
NM_001354901.1:c.5423T>A	NP_001341830.1:p.Phe1808Tyr
NM_001354901.2:c.5423T>A	NP_001341830.1:p.Phe1808Tyr
NM_001354902.1:c.5327T>A	NP_001341831.1:p.Phe1776Tyr
NM_001354902.2:c.5327T>A	NP_001341831.1:p.Phe1776Tyr
NM_001354903.1:c.5297T>A	NP_001341832.1:p.Phe1766Tyr
NM_001354903.2:c.5297T>A	NP_001341832.1:p.Phe1766Tyr
NM_001354904.1:c.5222T>A	NP_001341833.1:p.Phe1741Tyr
NM_001354904.2:c.5222T>A	NP_001341833.1:p.Phe1741Tyr
NM_001354905.1:c.5120T>A	NP_001341834.1:p.Phe1707Tyr
NM_001354905.2:c.5120T>A	NP_001341834.1:p.Phe1707Tyr
NM_001354906.1:c.4751T>A	NP_001341835.1:p.Phe1584Tyr
NM_001354906.2:c.4751T>A	NP_001341835.1:p.Phe1584Tyr
ENST00000257430.8:c.5600T>A	ENSP00000257430.4:p.Phe1867Tyr
ENST00000504915.3:c.5654T>A	ENSP00000473355.2:p.Phe1885Tyr
ENST00000505350.2:c.*5606T>A	ENSP00000481752.1:n.*5606T>A
ENST00000507379.6:c.5546T>A	ENSP00000423224.2:p.Phe1849Tyr
ENST00000508376.6:c.5600T>A	ENSP00000427089.2:p.Phe1867Tyr
ENST00000508624.5:c.*4922T>A	ENSP00000424265.1:n.*4922T>A
ENST00000509732.6:c.5600T>A	ENSP00000426541.2:p.Phe1867Tyr
ENST00000512211.7:c.5600T>A	ENSP00000423828.3:p.Phe1867Tyr
ENST00000520401.1:c.230+12222T>A